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Pravastatin sodium

NDC 55111-229, Pravastatin sodium, tablet, from Dr.Reddy's Laboratories Limited.

Product NDC
55111-229
Status
Listed
Labeler
Dr.Reddy's Laboratories Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076714
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55111-229 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRAVASTATIN SODIUM10 mg/1

Pharmacologic classes

HMG-CoA Reductase Inhibitor [EPC]; Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

Package NDCNDC-11Package
55111-229-0155111022901100 TABLET in 1 BOTTLE (55111-229-01)
55111-229-0555111022905500 TABLET in 1 BOTTLE (55111-229-05)
55111-229-305511102293030 TABLET in 1 BOTTLE (55111-229-30)
55111-229-905511102299090 TABLET in 1 BOTTLE (55111-229-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/99cc0546-bb2d-751e-edfd-1c15a1182e0c

Use it

Look up 55111-229 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55111-229 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55111-229. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.